Welcome to Haleon

We’re a purpose-driven, world-class consumer company putting everyday health in the hands of millions. In just three years since our launch, we’ve grown, evolved and are now entering an exciting new chapter – one filled with bold ambitions and enormous opportunity. Our trusted portfolio of brands – including Sensodyne®, Panadol®, Advil®, Voltaren®, Theraflu®, Otrivin®, and Centrum® – lead in resilient and growing categories. What sets us apart is our unique blend of deep human understanding and trusted science.

Now it’s time to fully realise the full potential of our business and our people. We do this through our Win as One strategy. It puts our purpose – to deliver better everyday health with humanity – at the heart of everything we do. It unites us, inspires us, and challenges us to be better every day, driven by our agile, performance-focused culture.

Job Purpose

Are you energised by the opportunity to partner with key leaders in global medical science to enhance global operational support? If so, this Clinical Study Management Manager role could be an exciting opportunity to explore.

The role provides operational leadership to the Clinical Study Team and is responsible for the planning, management, execution and delivery of the trial according to study timelines, budget and quality. The role will require robust use of project management tools and operational practices.

Key Responsibilities

• Exhibits strong study operational strategy to plan and oversee execution of assigned studies, supporting clinical strategy defined in the Non-Clinical & Clinical Development Plan.
• Acts as Study Team Leader and primary operational contact for 1–3 trials of average design and protocol complexity, including clinical trials, behavioural testing, and decentralised/virtual trials.
• Has the ability and agility to manage the delivery of any type of study, including complex or unusual study designs, new indications, challenging regional environments and local regulations, while strategically influencing operational delivery.
• Responsible for the implementation, conduct and tracking of study trials in compliance with ICH/GCP and local regulations, company SOPs and written standards for the conduct of human subject research, study timelines, budget and project specifications.
• Provides operational and strategic leadership to assure successful delivery of trials, in alignment with Haleon expectations and behaviours.
• Provides oversight of clinical sites, CROs and vendor activities according to Functional Service Provider (FSP) or Full-Service Outsourcing (FSO) models.
• Leads or participates in clinical site assessments.
• Leads the coordination of cross-functional department activities to successfully achieve milestones and quality deliverables in study management, including study start-up, recruitment, study conduct, database lock and study close-out, with risk and issue management and assurance of TMF inspection readiness.
• Contributes to plans and study documents from an operational standpoint, such as protocols, informed consent forms, monitoring plans, vendor contracts and clinical study reports.
• Acts as HBS custodian.
• Takes on functional leadership responsibilities, providing expert consultation for issue resolution and piloting new ways of working.
• Represents Clinical Operations in vendor and due diligence/audit activities and provides subject matter expertise on implementing Good Clinical Practice, business improvement initiatives and change implementation.